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rs41552719

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41552719(A;A)
Make rs41552719(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354930
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41552719
ebirs41552719
HLIrs41552719
Exacrs41552719
Varsomers41552719
Maprs41552719
PheGenIrs41552719
hapmaprs41552719
1000 genomesrs41552719
hgdprs41552719
ensemblrs41552719
gopubmedrs41552719
geneviewrs41552719
scholarrs41552719
googlers41552719
pharmgkbrs41552719
gwascentralrs41552719
openSNPrs41552719
23andMers41552719
23andMe allrs41552719
SNP Nexus

SNPshotrs41552719
SNPdbers41552719
MSV3drs41552719
GWAS Ctlgrs41552719
Max Magnitude0
ClinVar
Risk rs41552719(A;A)
Alt rs41552719(A;A)
Reference rs41552719(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322707C>T
CLNSRC
CLNACC